The conjugates of ferrocene-1,1′-diamine and amino acids. A novel synthetic approach and conformational analysis-Reference-Cited by-同舟云学术

The conjugates of ferrocene-1,1′-diamine and amino acids. A novel synthetic approach and conformational analysis

Published:2015 Issue:37 Volume:44 Page:16405-16420
ISSN:1477-9226
Container-title:Dalton Transactions
language:en
Short-container-title:Dalton Trans.

Author:

Kovačević Monika¹²³⁴⁵,Kodrin Ivan⁶⁷³⁴⁵,Cetina Mario⁸⁹³⁴⁵,Kmetič Ivana¹²³⁴⁵,Murati Teuta¹²³⁴⁵,Semenčić Mojca Čakić¹²³⁴⁵,Roca Sunčica¹⁰¹¹⁴⁵,Barišić Lidija¹²³⁴⁵

Affiliation:

1. Department of Chemistry and Biochemistry

2. Faculty of Food Technology and Biotechnology

3. University of Zagreb

4. Zagreb

5. Croatia

6. Department of Chemistry

7. Faculty of Science

8. Department of Applied Chemistry

9. Faculty of Textile Technology

10. NMR Centre

11. Ruđer Bošković Institute

Abstract

The first example of an orthogonally protected ferrocene-1,1′-diamine based peptidomimetic with a stable intramolecular hydrogen bond pattern comprised of two β-turns is reported.

Funder

Hrvatska Zaklada za Znanost

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/DT/C5DT01610J

Reference94 articles.

1. Turns in Peptides and Proteins

2. Roles of β-turns in protein folding: From peptide models to protein engineering

3. Structural characterization of a -turn mimic within a protein-protein interface